Rabbit anti-β-Tubulin Monoclonal Antibody

WB result of β-Tubulin Rabbit mAb Primary antibody: β-Tubulin Rabbit mAb at 1/1000 dilution Lane 1: Hela whole cell lysate 20 µg Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 55 kDa Observed MW: 55 kDa Exposure time: 15 seconds

WB result of β-Tubulin Rabbit mAb Primary antibody: β-Tubulin Rabbit mAb at 1/1000 dilution Lane 1:Mouse brain lysate 20 µg Lane 2: NIH/3T3 whole cell lysate 20 µg Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 55 kDa Observed MW: 55 kDa Exposure time: Lane 1: 6 seconds; Lane 2: 15s

IHC shows positive staining in paraffin-embedded human testis. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human cerebral cortex. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded mouse liver. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded rat kidney. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

ICC shows cytoplasm staining in HeLa cells. Anti-β-tubulin antibody was used at 1/250 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution.The cells were fixed with 100% Methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were countersained with DAPI.

ICC shows cytoplasm staining in NIH3T3 cells. Anti-β-tubulin antibody was used at 1/250 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution.The cells were fixed with 100% Methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were countersained with DAPI.

Flow cytometric analysis of HeLa cells labelling β-tubulin antibody at 1/500 (0.1ug) dilution/ (red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Secondary antibody：#abs20025.

IHC shows positive staining in paraffin-embedded human testis. 

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. 

Counterstained with hematoxylin.              

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human placenta.

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human cerebral cortex.

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. 

Counterstained with hematoxylin. 

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human colon cancer. 

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. 

Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded mouse liver. 

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded rat kidney.

Anti-β-tubuLin antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

WB resuLt of β-TubuLin Rabbit mAb                                  

Primary antibody: β-TubuLin Rabbit mAb at 1/1000 dilution
Lane 1: Hela whole cell lysate 20 µg

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 50 kDa
Observed MW: 52 kDa
econds

WB resuLt of β-TubuLin Rabbit mAb
Primary antibody: β-TubuLin Rabbit mAb at 1/1000 dilution
Lane 1:Mouse brain lysate 20 µg
Lane 2: NIH/3T3 whole cell lysate 20 µg

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 50 kDa
Observed MW: 52 kDa

WB resuLt of β-TubuLin Rabbit mAb                

Primary antibody: β-TubuLin Rabbit mAb at 1/1000 dilution
Lane 1:rat brain lysate 20 µg

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 50 kDa
Observed MW: 52 kDa

Flow cytometric analysis of HeLa cells labelling β-tubuLin antibody at 1/500 (0.1ug) dilution/ (red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody. 

WB resuLt of β-TubuLin Rabbit mAb 
Primary antibody: β-TubuLin Rabbit mAb at 1/10000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: NIH/3T3 whole cell lysate 20 µg
Lane 3: rat brain lysate 20 µg
Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 50 kDa
Observed MW: 52 kDa

ICC shows positive staining in HeLa cells. Anti-β-tubuLin antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue).